Annika Winbo

Kontakt

Verksam som

Assistent klinisk vid Institutionen för folkhälsa och klinisk medicin

Byggnad 1A, plan 4, målpunkt B41, Norrlands universitetssjukhus Umeå universitet, 901 85 Umeå

Effects of cohort, genotype, variant, and maternal β-blocker treatment on foetal heart rate predictors of inherited long QT syndrome

Europace, Oxford University Press 2023, Vol. 25, (11)

Kaizer, Alexander M.; Winbo, Annika; Clur, Sally-Ann B; et al.

Cardiac response to water activities in children with Long QT syndrome type 1

PLOS ONE, Public Library of Science (PLoS) 2023, Vol. 18, (12)

Lundström, Anna; Wiklund, Urban; Winbo, Annika; et al.

To Modify or Not to Modify: Allele-Specific Effects of 3’UTR-KCNQ1 Single Nucleotide Polymorphisms on Clinical Phenotype in a Long QT 1 Founder Population Segregating a Dominant-Negative Mutation

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, American Heart Association 2022, Vol. 11, (18)

Winbo, Annika; Diamant, Ulla-Britt; Persson, Johan; et al.

LQTS founder population in Northern Sweden – the natural history of a potentially fatal inherited cardiac disorder

Biodemography and Social Biology, Routledge 2021, Vol. 66, (3-4) : 191-207

Diamant, Ulla-Britt; Winbo, Annika; Marcus, Karlsson; et al.

Functional hyperactivity in long OT syndrome type 1 pluripotent stem cell-derived sympathetic neurons

American Journal of Physiology. Heart and Circulatory Physiology, American Physiological Society 2021, Vol. 321, (1) : H217-H227

Winbo, Annika; Ramanan, Suganeya; Eugster, Emily; et al.

Fetal heart rate and arrhythmia profile predicts long QT syndrome (LQTS) genotype: Results of an 8-center international study

American Journal of Obstetrics and Gynecology, MOSBY-ELSEVIER 2018, Vol. 218, (1) : S93-S93

Cuneo, Bettina; Clur, Sally Ann; Swan, Heikki; et al.

Fetal heart rate reflects mutation burden and clinical outcome in twin probands with KCNQ1 mutations

HeartRhythm case reports, Vol. 4, (6) : 237-240

Winbo, Annika; Rydberg, Annika

Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations: a pedigree-based measured genotype association analysis

BMC Medical Genetics, Vol. 18

Winbo, Annika; Stattin, Eva-Lena; Westin, Ida Maria; et al.

Convergence of models of human ventricular myocyte electrophysiology after global optimization to recapitulate clinical long QT phenotypes

Journal of Molecular and Cellular Cardiology, Vol. 100 : 25-34

Mann, Stefan A.; Imtiaz, Mohammad; Winbo, Annika; et al.

Third Trimester Fetal Heart Rate Predicts Phenotype and Mutation Burden in the Type 1 Long QT Syndrome

Circulation: Arrhythmia and Electrophysiology, Vol. 8, (4) : 806-814

Winbo, Annika; Fosdal, Inger; Lindh, Maria; et al.

Vestibular dysfunction is a clinical feature of the Jervell and Lange-Nielsen Syndrome

Scandinavian Cardiovascular Journal, Vol. 49, (1) : 7-13

Winbo, Annika; Rydberg, Annika

Phenotype, origin and estimated prevalence of a common long QT syndrome mutation: a clinical, genealogical and molecular genetics study including Swedish R518X/KCNQ1 families

BMC Cardiovascular Disorders, BioMed Central 2014, Vol. 14 : 22-

Winbo, Annika; Stattin, Eva-Lena; Nordin, Charlotte; et al.

Vectorcardiographic recordings of the Q-T interval in a pediatric long Q-T syndrome population

Pediatric Cardiology, Vol. 34, (2) : 245-249

Diamant, Ulla-Britt; Jensen, Steen M; Winbo, Annika; et al.

Electrophysiological phenotype in the LQTS mutations Y111C and R518X in the KCNQ1 gene

Journal of applied physiology, American Physiological Society 2013, Vol. 115, (10) : 1423-1432

Diamant, Ulla-Britt; Vahedi, Farzad; Winbo, Annika; et al.

Iron-deficiency anaemia, gastric hyperplasia, and elevated gastrin levels due to potassium channel dysfunction in the Jervell and Lange-Nielsen Syndrome

Cardiology in the Young, Cambridge University Press 2013, Vol. 23, (3) : 325-334

Winbo, Annika; Sandström, Olof; Palmqvist, Richard; et al.

Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing

BMC Cardiovascular Disorders, BioMed Central 2012, Vol. 12 : 95-

Stattin, Eva-Lena; Boström, Ida Maria; Winbo, Annika; et al.

Long QT syndrome in Sweden: founder effects and associated cardiac phenotypes

Umeå University medical dissertations, 1515

Winbo, Annika

Prevalence, mutation spectrum, and cardiac phenotype of the Jervell and Lange-Nielsen syndrome in Sweden

Europace, Vol. 14, (12) : 1799-1806

Winbo, Annika; Stattin, Eva-Lena; Diamant, Ulla-Britt; et al.

Origin of the Swedish long QT syndrome Y111C/KCNQ1 founder mutation

Heart Rhythm, Elsevier 2011, Vol. 8, (4) : 541-547

Winbo, Annika; Diamant, Ulla-Britt; Rydberg, Annika; et al.

Two automatic QT algorithms compared with manual measurement in identification of long QT syndrome

Journal of Electrocardiology, Vol. 43, (1) : 25-30

Diamant, Ulla-Britt; Winbo, Annika; Stattin, Eva-Lena; et al.

Low incidence of sudden cardiac death in a Swedish Y111C type 1 long-QT syndrome population

Circulation: Cardiovascular Genetics, Philadelphia, PA: Lippincott Williams & Wilkins 2009, Vol. 2, (6) : 558-564

Winbo, Annika; Diamant, Ulla-Britt; Stattin, Eva-Lena; et al.

The Swedish long QT syndrome R518X/KCNQ1 founder population- origin and clinical phenotype: phenotypic variability partly explained by gender-specific effects of sequence variants in the NOS1AP gene

Winbo, Annika; Stattin, Eva-Lena; Norberg, Anna; et al.

Visa publikationer i DiVA

Forskargrupper

Gruppmedlem

Centrum för kardiovaskulär genetik